510(k) K241702 ยท DQX Wire, Guide, Catheter
CROSSLEAD 0.014inch
| Applicant | Asahi Intecc Co., Ltd., Seto, JP |
| Decision | Substantially Equivalent, Feb 6, 2025 |
| Received | Jun 13, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K241702
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.